A career with MilliporeSigma is an ongoing journey of discovery: our 50,000 people are shaping how the world lives, works and plays through next generation advancements in healthcare, life science and performance materials. For 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others. MilliporeSigma is a business of Merck KGaA, Darmstadt, Germany.
Who we are:
MilliporeSigma is the North American life science brand of Merck KGaA, Darmstadt, Germany – a leading science and technology company. It offers a broad range of innovative products and services to biotech and pharmaceutical drug therapies businesses. Through dedicated collaboration with the scientific and engineering communities, and as one of the top three R&D investors in the life science tools industry, the brand serves as a strategic partner to customers and helps advance the promise of life science.
MilliporeSigma is seeking to hire a Senior Scientist in the Reference Materials R&D Innovation Department at Cerilliant’s Corporation site in Round Rock TX. The Cerilliant site manufactures high quality quantitative chemical reference standards for a diverse group of industries including forensic/toxicology, clinical/toxicology, clinical chemistry, pharmaceuticals, natural health products, environmental and food. The Innovation Department is responsible for new product and capabilities development to support growth of the business.
In this role, you will be responsible for development and validation of methods, and products in support of Cerilliant new products and innovation pipeline. You will work collaboratively with the innovation and new product teams across departments on multiple aspects of product design, method development, tech-transfer, stability, manufacture and testing. You must be independent, driven and motivated to both learn from others, and effectively transfer knowledge and processes to others. You must have demonstrated ability to effectively manage your time and to manage multiple projects. Excellent written and verbal communication skills and ability to interact and collaborate with peers are critical to success in this role.
All work is performed in compliance with Cerilliant quality and safety policies, and good housekeeping practices.
Who You Are:
Extensive technical expertise and experience in LC-MS/MS method development, validation and analysis, preferably in clinical or bioanalytical environment
Knowledge of HPLC method development and other analytical/organic chemistry techniques
Demonstrated motivation, ability to learn new techniques, and to collaborate well with others
PhD with minimum 2 years relevant experience or MS/BS with minimum 5-7 years relevant experience; in analytical, organic, bioorganic or pharmaceutical fields.
Experience with bioanalytical methods preferred
Experience working under regulated quality system requirements for GMPs, GLPs, ISO and other regulatory requirements preferred
Experience with product development preferred
Working knowledge of Cerilliant products, their applications and customer requirements preferred
ADDITIONAL LOCAL NEEDS:
Comfortable working in chemical manufacturing facility and handling various chemicals including organic, inorganic, volatiles, acids, and bases. Comfortable working with biological matrices e.g. serum, urine etc. Requires routine use of PPE including but not limited to: gloves, scrubs, lab coat, face shield, respirator. Routine use of engineering controls including fume hoods and glove boxes. Physical Requirements: Hearing, vision within normal limits. May sit at PC for periods of time. May stand working at a bench for long periods of time
Other Information: - The above description covers the most significant job duties and does not exclude other work assignments not mentioned.
What we offer:
With us, there are always opportunities to break new ground. We empower you to fulfil your ambitions, and our diverse businesses offer various career moves to seek new horizons. We trust you with responsibility early on and support you to draw your own career map that is responsive to your aspirations and priorities in life. Join us and bring your curiosity to life!
Apply and find more information at come2emd.com
The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to his/her Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because he/she made a good faith report of discrimination.
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Website : http://www.merckmillipore.com
Our purpose is to solve the toughest problems in life science by collaborating with the global scientific community – and through that, we aim to accelerate access to better health for people everywhere. We provide scientists and engineers with best-in-class lab materials, technologies and services. With the 2015 combination of Merck Millipore and Sigma-Aldrich, we now have a broad portfolio of 300,000 products, an expanded global footprint and an industry-leading eCommerce platform - SigmaAldrich.com. We are dedicated to making research and biotech production simpler, faster and safer.